A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980345



Internal ID54271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28258557..28258557hg38UCSC Ensembl
chr6:28226335..28226335hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5534427
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980345
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03872


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